Chromium-based catalysts and processes for converting alkanes into higher and lower aliphatic hydrocarbons

Patent metadata

Field	Value
Publication number	US-11603339-B2
Application number	US-202217847303-A
Country	US
Kind code	B2
Filing date	Jun 23, 2022
Priority date	Sep 16, 2019
Publication date	Mar 14, 2023
Grant date	Mar 14, 2023

Abstract

Processes for cracking an alkane reactant to form a lower aliphatic hydrocarbon product and for converting an alkane reactant into a higher aliphatic hydrocarbon product are disclosed, and these processes include a step of contacting the alkane reactant with a supported chromium (II) catalyst. In addition to the formation of various aliphatic hydrocarbons, such as linear alkanes, branched alkanes, 1-alkenes, and internal alkenes, aromatic hydrocarbons and hydrogen also can be produced.

First claim

We claim:

1. A process for cracking an alkane reactant to form a lower aliphatic hydrocarbon product, the process comprising:
contacting the alkane reactant with a supported chromium (II) catalyst to form the lower aliphatic hydrocarbon product, wherein the lower aliphatic hydrocarbon product has a molecular weight less than that of the alkane reactant; wherein:
the alkane reactant comprises a C n alkane compound;
the lower aliphatic hydrocarbon product comprises a (C n-1 )− aliphatic hydrocarbon compound;
n is an integer from 2 to 36; and
the lower aliphatic hydrocarbon product is formed at a temperature from about 10° C. to about 350° C.

2. The process of claim 1 , wherein the alkane reactant comprises ethane, propane, butane, pentane, hexane, heptane, octane, nonane, decane, undecane, dodecane, tridecane, tetradecane, pentadecane, hexadecane, heptadecane, octadecane, or any combination thereof.

3. The process of claim 1 , wherein contacting the alkane reactant with the supported chromium (II) catalyst forms the lower aliphatic hydrocarbon product and:
H 2 ;
an isomer of the alkane reactant;
an aromatic compound;
a higher aliphatic hydrocarbon product, wherein the higher aliphatic hydrocarbon product has a molecular weight greater than that of the alkane reactant; or
any combination thereof.

4. The process of claim 1 , wherein:
the lower aliphatic hydrocarbon product is formed at a temperature from about 20° C. to about 300° C.; and
a conversion of the alkane reactant is at least about 10 wt. %.

5. The process of claim 1 , wherein:
the supported chromium (II) catalyst contains from about 0.01 to about 50 wt. % of chromium, based on the weight of the supported chromium (II) catalyst; and
the supported chromium (II) catalyst contains chromium having an average valence of less than or equal to 3.

6. The process of claim 1 , wherein the process comprises contacting the alkane reactant with a fluidized bed of the supported chromium (II) catalyst.

7. The process of claim 1 , wherein the process comprises contacting the alkane reactant with a fixed bed of the supported chromium (II) catalyst.

8. The process of claim 1 , wherein the supported chromium (II) catalyst contains chromium having an average valence of less than or equal to 3.

9. The process of claim 1 , wherein the supported chromium (II) catalyst comprises a solid oxide, a chemically-treated solid oxide, a zeolite, or a combination thereof.

10. The process of claim 1 , wherein a conversion of the alkane reactant is at least about 10 wt. %.

11. The process of claim 1 , wherein contacting the alkane reactant with the supported chromium (II) catalyst forms the lower aliphatic hydrocarbon product and H 2 .

12. The process of claim 1 , wherein contacting the alkane reactant with the supported chromium (II) catalyst forms the lower aliphatic hydrocarbon product and an isomer of the alkane reactant.

13. The process of claim 1 , wherein contacting the alkane reactant with the supported chromium (II) catalyst forms the lower aliphatic hydrocarbon product and an aromatic compound.

14. The process of claim 1 , further comprising:
forming an effluent comprising the lower aliphatic hydrocarbon product; and
separating at least a portion of the alkane reactant from the effluent, and wherein the at least a portion of the alkane reactant is recycled and contacted with the supported chromium (II) catalyst again.

15. The process of claim 1 , further comprising a step of regenerating at least a portion of the supported chromium (II) catalyst.

16. A process for cracking an alkane reactant to form a lower aliphatic hydrocarbon product, the process comprising:
contacting the alkane reactant with a supported chromium (II) catalyst to form the lower aliphatic hydrocarbon product, wherein the lower aliphatic hydrocarbon product has a molecular weight less than that of the alkane reactant;
wherein contacting the alkane reactant with the supported chromium (II) catalyst forms the lower aliphatic hydrocarbon product and a higher aliphatic hydrocarbon product, wherein the higher aliphatic hydrocarbon product has a molecular weight greater than that of the alkane reactant.

17. A process for cracking an alkane reactant to form a lower aliphatic hydrocarbon product, the process comprising:
contacting the alkane reactant with a supported chromium (II) catalyst to form the lower aliphatic hydrocarbon product, wherein the lower aliphatic hydrocarbon product has a molecular weight less than that of the alkane reactant;
wherein the lower aliphatic hydrocarbon product is formed at a temperature from about 20° C. to about 300° C.

18. The process of claim 17 , wherein the alkane reactant comprises a C 2 to C 18 alkane compound.

19. A process for cracking an alkane reactant to form a lower aliphatic hydrocarbon product, the process comprising:
reducing a supported chromium (VI) catalyst with carbon monoxide to form a supported chromium (II) catalyst; and
contacting the alkane reactant with the supported chromium (II) catalyst to form the lower aliphatic hydrocarbon product, wherein the lower aliphatic hydrocarbon product has a molecular weight less than that of the alkane reactant.

20. The process of claim 19 , wherein the alkane reactant comprises a C 2 to C 18 alkane compound.

Assignees

• Chevron Phillips Chemical Co Lp

Inventors

• Cruz Carlos A
• Mcdaniel Max P
• Monwar Masud M
• Barr Jared

Classifications

• B01J35/40

  characterised by dimensions, e.g. grain size (in a colloidal state B01J35/23; crystallite size B01J35/77) · CPC title

• C10G11/02

  characterised by the catalyst used · CPC title

• B01J38/00

  Regeneration or reactivation of catalysts, in general · CPC title

• B01J37/08

  Heat treatment {(B01J37/0009, B01J37/0018 take precedence)} · CPC title

• B01J37/16

  Reducing · CPC title